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J. Biol. Chem., Vol. 275, Issue 38, 29299-29307, September 22, 2000
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§¶,
,
, and
**
From the We have characterized the structure of a sulfated
D-galactan from the red algae Botryocladia
occidentalis. The following repeating structure
(-4-
Laboratório de Tecido Conjuntivo,
Hospital Universitário Clementino Fraga Filho and Departamento de
Bioquímica Médica, Centro de Ciências da
Saúde, Universidade Federal do Rio de Janeiro, Caixa Postal
68041, Rio de Janeiro, 21941-590 Brazil, the
§ Departamento de Engenharia de Pesca, Universidade Federal
do Ceará, Caixa Postal 12168, Fortaleza, Ceará,
60365-000, Brazil, and the
Centro Nacional de Ressonância
Nuclear Magnética de Macromoléculas, Departamento de
Bioquímica Médica, Universidade Federal do Rio de
Janeiro, Rio de Janeiro, 21941-590, Brazil
-D-Galp-1
3-
-D-Galp-1
)
was found for this polysaccharide, but with a variable sulfation
pattern. Clearly one-third of the total
-units are
2,3-di-O-sulfated and another one-third are 2-O-sulfated. The algal sulfated D-galactan has
a potent anticoagulant activity (similar potency as unfractionated
heparin) due to enhanced inhibition of thrombin and factor Xa by
antithrombin and/or heparin cofactor II. We also extended the
experiments to several sulfated polysaccharides from marine
invertebrates with simple structures, composed of a single repeating
structure. A 2-O- or 3-O-sulfated L-galactan (as well as a 2-O-sulfated
L-fucan) has a weak anticoagulant action when compared with
the potent action of the algal sulfated D-galactan.
Possibly, the addition of two sulfate esters to a single
-galactose
residue has an "amplifying effect" on the anticoagulant action,
which cannot be totally ascribed to the increased charge density of the
polymer. These results indicate that the wide diversity of
polysaccharides from marine alga and invertebrates is a useful tool to elucidate structure/anticoagulant activity relationships.
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